No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
100 (estimated)
Sponsor
Zealand University Hospital · Other
Who this trial is looking for
This trial is looking for stroke survivors living in the community to test a 12-week program aimed at reducing sedentary behavior and increasing physical activity. Participants will receive motivational interviews to help set goals and plan actions in their daily life after stroke.
Are You a Good Fit for This Trial?
You may be able to join if
I have had a stroke
I am able to walk independently
I can speak and understand Danish
I was discharged with a rehabilitation plan within 1-14 days after my hospitalization
My modified rankin score is between 1 and 3 at discharge
You may not be able to join if
I have difficulty speaking or understanding language (aphasia)
I cannot give informed consent
I am unable to walk independently
I have a mental illness
I have a serious health condition like terminal cancer
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This randomized control trial (RCT) aims to test the effect of a 12 weeks tailored behavioral intervention on stroke survivors living in the community and compare the results to a control group of stroke survivors participating in standard care. The intervention's purpose is to lower the time spend with sedentary behavior and raise the level of physical activity in stroke survivors throughout thei…
This randomized control trial (RCT) aims to test the effect of a 12 weeks tailored behavioral intervention on stroke survivors living in the community and compare the results to a control group of stroke survivors participating in standard care. The intervention's purpose is to lower the time spend with sedentary behavior and raise the level of physical activity in stroke survivors throughout their everyday life. The intervention contains two motivational interviews with a focus on goal setting, action planning, motivation, fatigue management, and general information on life after stroke. The primary outcome for behavior change is objectively measured physical activity using an activity tracker (ActivPal4 Micro) and secondary glycohemoglobin and changes in quality of life.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* Verified ischemic stroke or intracerebral hemorrhage
* Modified rankin score (mRS) 1-3 at discharge
* Discharged with at rehabilitation plan within 1-14 hospitalization days
* Able to ambulate independently
* Speak and understand Danish
Exclusion Criteria:
* Aphasia
* Unable…
Inclusion Criteria:
* Verified ischemic stroke or intracerebral hemorrhage
* Modified rankin score (mRS) 1-3 at discharge
* Discharged with at rehabilitation plan within 1-14 hospitalization days
* Able to ambulate independently
* Speak and understand Danish
Exclusion Criteria:
* Aphasia
* Unable to give informed consent
* Unable to ambulate independently
* Mental illness
* Other co-morbidity like terminal cancer.
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